Sochor H
Kardiologischen Universitätsklinik Wien.
Acta Med Austriaca Suppl. 1989;39:1-36.
The assessment of myocardial viability following interventions aiming at restitution of antegrade blood flow by PTCA and thrombolysis has become one of the most important goals to judge interventional success. Conventional markers as ECG, the extent of the regional wall motion abnormality and enzymes have conceptual limitations. We had shown previously that increased residual glucose metabolism in reperfused myocardium can be assessed by F-18 2-deoxy-glucose (FDG) and positron emission tomography (PET) and will predict functional recovery in reperfused myocardium. The present study introduces a novel concept for the evaluation of myocardial viability by the application of multiple tracer techniques and investigates tracer behaviour in relation to blood flow, regional wall motion, coronary anatomy and histology. The experimental data compare segmental uptake of F-18 FDG with the current most clinically important perfusion marker Tl-201 and Tc-99m (Sn) pyrophosphate (Tc-99mPPi) as a marker of myocardial necrosis in a canine model following a 3 hour intracoronary balloon occlusion and subsequent reperfusion and therefore in a clinically attributable occlusion and reperfusion scenario. Myocardial blood flow was assessed by microspheres, regional fractional tracer retention fractions were evaluated from tissue tracer concentrations, the arterial input function and quantitative blood flow measurements. The extent of ischemic damage was evaluated by TTC post mortem staining, histology, and histochemistry. Additional studies to illucidate the mechanism of increased glucose utilization were done by analysis of other substrates as lactate. The result within the area at risk was assessed in relation to the metabolic behaviour. PET methods were validated in the same dog model as a quantitative biochemical in-vivo assay and imaging procedure and demonstrate the ability of this noninvasive techniques to measure blood flow and myocardial metabolism, especially exogenous glucose utilization. Time dependent and repetitive PET studies may indicate a delayed recovery of myocardial metabolism following an ischemic event with a pattern of a blood flow-metabolism mismatch, characteristic for persistent viability. Metabolic data by imaging correlate with reference techniques as arterio-venous sampling and post mortem histochemical staining method using TTC, PAS, and glycogen techniques. The clinical part applies the proposed tracer concept to patients with acute myocardial infarction and following reperfusion interventions as well using conventional markers and again positron markers. These studies indicate possibilities to assess myocardial viability by the same simultaneou
通过经皮冠状动脉腔内血管成形术(PTCA)和溶栓恢复顺行血流的干预措施后,评估心肌活力已成为判断介入治疗成功与否的最重要目标之一。传统指标如心电图、局部室壁运动异常程度和酶类存在概念上的局限性。我们之前已经表明,再灌注心肌中残余葡萄糖代谢增加可通过F-18 2-脱氧葡萄糖(FDG)和正电子发射断层扫描(PET)进行评估,并且可以预测再灌注心肌的功能恢复。本研究引入了一种通过应用多种示踪技术评估心肌活力的新概念,并研究示踪剂行为与血流、局部室壁运动、冠状动脉解剖结构和组织学的关系。实验数据在犬模型中比较了F-18 FDG的节段摄取与目前临床上最重要的灌注标记物铊-201(Tl-201)以及锝-99m(锡)焦磷酸盐(Tc-99mPPi)(作为心肌坏死的标记物),该犬模型经历了3小时冠状动脉内球囊闭塞及随后的再灌注,因此处于临床上可归因的闭塞和再灌注情况。通过微球评估心肌血流,从组织示踪剂浓度、动脉输入函数和定量血流测量中评估局部示踪剂保留分数。通过死后TTC染色、组织学和组织化学评估缺血损伤的程度。通过分析其他底物如乳酸进行了额外的研究以阐明葡萄糖利用增加的机制。在危险区域内的结果根据代谢行为进行评估。PET方法在与定量生化体内测定和成像程序相同的犬模型中得到验证,并证明了这种非侵入性技术测量血流和心肌代谢的能力,特别是外源性葡萄糖利用。时间依赖性和重复性PET研究可能表明缺血事件后心肌代谢的延迟恢复,呈现出血流-代谢不匹配的模式,这是持续存活的特征。通过成像获得的代谢数据与参考技术相关,如动静脉采样以及使用TTC、PAS和糖原技术的死后组织化学染色方法。临床部分将所提出的示踪剂概念应用于急性心肌梗死患者以及再灌注干预后的患者,同时使用传统标记物和正电子标记物。这些研究表明了通过相同的同时……(原文此处不完整)